Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Just Diagnosed!


sweetpomme

Recommended Posts

sweetpomme Newbie

Hi everyone :)

I am 26 years old and was just diagnosed with Celiac Disease, I plan on meeting with a nutritionist soon.

I was wondering how you made the changes with your diet - did you change all of your diet at once or did you slowly change your eating habits?

thank you and talk to you soon !! :)


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



nvsmom Community Regular

Hi everyone :)

I am 26 years old and was just diagnosed with Celiac Disease, I plan on meeting with a nutritionist soon.

I was wondering how you made the changes with your diet - did you change all of your diet at once or did you slowly change your eating habits?

thank you and talk to you soon !! :)

Welcome to the board.

 

I changed my diet as soon as possible. I did not finish off any gluten products but gave them away instead.  It took me about a week to be sure that my home was gluten-free.

julissa Explorer

I too went cold turkey. learned as much as I could about hidden gluten, things to look for in ingredients. I slowly started changing over my kitchen. everything I learned, I learned about here. read, read, read.

 

good luck! 

bartfull Rising Star

Yep. The sooner you quit, the sooner you will be healthy again. Do go to the Newbie 101 thread in the coping section here to learn how to avoid cross-contamination and so much more.

 

It may sound crazy, but congratulations on your diagnosis. You can now control your health without surgery or medication. A simple change in your diet and you can avoid the complications so many of us have been through.

ravenwoodglass Mentor

Agree with the others. You need to stop not taper. Tapering off will not make the process any easier and will keep the antibodies and thus your symptoms active. 

Welcome to the board.  Hope your feeling better soon. 

CathyO Rookie

I am 60 and was diagnosed just this year.

 

I was so sick that I immediately cleaned out my entire pantry. Donated any foods with gluten. Got a new toaster. Threw away all my wooden spoons, etc. etc.  I was terrified to eat any gluten, because all accidental gluten exposure made me extremely ill.  I ate at home all the time for probably the first 3-4 months. 

 

I'm still very cautious about eating out.

 

I do have a 12 year old at home, and he has a small bottom shelf area in the pantry for some snacks. We have established strict rules about foods with gluten and where he can eat them and what he needs to do to clean up after himself.

 

All the meals we prepare for the family are gluten-free.

I'm kind of an all or nothing kind of person when it comes to gluten-free.

 

I've learned a lot from reading online, and even more in this group. 

sweetpomme Newbie

Thank you everyone for your help! I thought it would be easier for me to make changes slowly but as I'm reading your advice, it feels like it's going to be easier to do it all at once, especially with all the precautions needed to avoid the cross-contamination. I am reading a lot of posts on the forum today and rented a few books about getting gluten-free. Did any of you consult a nutritionist, or did you just get all the information needed in books/internet?


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



CathyO Rookie

Thank you everyone for your help! I thought it would be easier for me to make changes slowly but as I'm reading your advice, it feels like it's going to be easier to do it all at once, especially with all the precautions needed to avoid the cross-contamination. I am reading a lot of posts on the forum today and rented a few books about getting gluten-free. Did any of you consult a nutritionist, or did you just get all the information needed in books/internet?

My education has been books, this site, a few other sites and other people I know with Celiac.

I live in a pretty rural area with a teeny hospital. There's not a nutritionist who works with celiac disease within a couple hours of me.

If you have access to a nutritionist who can help? I'd go for it. Knowledge is power, and the more you know the easier this change will be for you.

nvsmom Community Regular

Thank you everyone for your help! I thought it would be easier for me to make changes slowly but as I'm reading your advice, it feels like it's going to be easier to do it all at once, especially with all the precautions needed to avoid the cross-contamination. I am reading a lot of posts on the forum today and rented a few books about getting gluten-free. Did any of you consult a nutritionist, or did you just get all the information needed in books/internet?

 

Unless your nutritionist is knowledgeable on celiac disease or the gluten-free diet, they may not be a lot of help.  I've heard very mixed reviews on seeing a nutritionist.

 

Basically, for me it boiled down to the fact that it is healthier to limit your gluten-free substitute foods as they tend to be less healthy than wheat flour foods.  For example, prepackaged gluten-free bread is generally less healthy than normal bread because most flours are fortified with vitamins and tend to have a bit more fibre. Also gluten-free baked items tend to have a higher glycemic index and convert to sugar very quickly in our bodies.

 

Usually the healthiest option is to not replace your "glutenous" foods.  If you are having cheese and meat sandwich, then skip the bread and just eat the insides or use a rice wrap.  Noodles can be substituted with rice noodles but an even healthier solution is spaghetti squash. gluten-free muffin mixes are often like dry cupcakes; its better to use almond or coconut flour and skip the rice flours and starches when you can.... You see what I mean?

 

If you read a few books, I'm sure you'll find most of what you need, including a list of unsafe ingredients like this one:https://www.celiac.com/celiac-disease/forbidden-gluten-food-list-unsafe-ingredients-r182/  It is handy to carry a list like this around in the first few months.

 

Also, about half of all celiacs are lactose intolerant while they are healing during the first 6 months or so.  It is often a good idea to skip dairy if you feel that you are still having problems.

 

The first few months are definitely the hardest.  Just hang in there.  :)

SMRI Collaborator

I stopped as soon as my GI told me to.  I was diagnosed in June but they told me to wait until July after follow-up appointments to stop in case they needed to do more testing.  I spend most of July eating things I knew I couldn't have any longer LOL :D.

 

I went to a nutritionist.  She was helpful but I have gotten more information from this site.  After my visit I discovered that she was not covered under my insurance so it's kind of wasted money unfortunately. I'd double check your insurance just in case.

notme Experienced

here is some very helpful info:

 

https://www.celiac.com/forums/topic/91878-newbie-info-101/

 

i was recommended to see a dietitian - insurance would pay - called for an appointment:  sure, see ya in 2 weeks...  

 

*blink*  what?  sooo, what am i supposed to eat for two weeks??!!  my husband googled and he found this site.  i cancelled my appointment a few days later.  pretty glad i did being as the next time i went to my g.p. for my blood pressure check-up, the nurse practitioner didn't even know what celiac was.  she looked at me all stupid when i said i replaced my lip gloss and said, "what do you do?  eat it?"  o, boy   <_< so, personally, i have better faith in people who actually have to live gluten free every day.

 

welcome and good luck  :)

CathyO Rookie

here is some very helpful info:

 

https://www.celiac.com/forums/topic/91878-newbie-info-101/

 

i was recommended to see a dietitian - insurance would pay - called for an appointment:  sure, see ya in 2 weeks...  

 

*blink*  what?  sooo, what am i supposed to eat for two weeks??!!  my husband googled and he found this site.  i cancelled my appointment a few days later.  pretty glad i did being as the next time i went to my g.p. for my blood pressure check-up, the nurse practitioner didn't even know what celiac was.  she looked at me all stupid when i said i replaced my lip gloss and said, "what do you do?  eat it?"  o, boy   <_< so, personally, i have better faith in people who actually have to live gluten free every day.

 

welcome and good luck  :)

 

Wow. Not at the 2 weeks part, because around here it takes months to get an appointment with anyone for anything.

 

I see a nurse practitioner regularly, and I must say that mine is a lot more knowledgeable.  She's given me a lot of resources and talked about probiotics with me, and made suggestions to me.  She even reads things I bring her and thanks me for them. 

 

notme Experienced

i was very underweight i wonder if they worked me in?  i needed help before that, lolz!  i never have made an appointment with one before or since, so i don't know what is the norm. are you in the us, cathy?  i see my GI every 6 months and he knows his stuff.   their office is pretty good about letting me come in for tests without an appointment.  i just have to call ahead so they can pull my chart.   

CathyO Rookie

i was very underweight i wonder if they worked me in?  i needed help before that, lolz!  i never have made an appointment with one before or since, so i don't know what is the norm. are you in the us, cathy?  i see my GI every 6 months and he knows his stuff.   their office is pretty good about letting me come in for tests without an appointment.  i just have to call ahead so they can pull my chart.   

 

I am in the US.  A small rural area, with limited medical services.   It took 3 months to get an appointment with a GI locally.

Then another 3 months to schedule an endoscopy.  It's a nightmare.

1desperateladysaved Proficient

I did taper off gluten over a few days, longer if one counts the flavoring that I didn't read the label on.  My first tier was major food groups.  I didn't eat bread, or use any gluten flours in my cooking.  I got my kids to take certain large quantities of grains out of the kitchen.  There was a box of gluten in the pantry for a much longer time, but it wasn't being used.  Then I started being more concerned about cross contaminated goods in my food supply.  That meant I started calling companies about how they produced their products.  In this tier I checked my supplements, and had my family remove more grain products from the kitchen.  The next tier I checked my shampoo and conditioner (already gluten free!)  Oh, and last of all I checked pet foods, dish soaps, and laundry soap.  I recommend studying if you are in limbo or gluten challenge and beginning to switch minor products as soon as they need replacing.  Just don't forget to keep eating gluten until testing is done.

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,929
    • Most Online (within 30 mins)
      7,748

    Mike Rowicki
    Newest Member
    Mike Rowicki
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • lehum
      Hi and thank you very much for your detailed response! I am so glad that the protocol worked so well for you and helped you to get your health back on track. I've heard of it helping other people too. One question I have is how did you maintain your weight on this diet? I really rely on nuts and rice to keep me at a steady weight because I tend to lose weight quickly and am having a hard time envisioning how to make it work, especially when not being able to eat things like nuts and avocados. In case you have any input, woud be great to hear it! Friendly greetings.
    • Hmart
      I was not taking any medications previous to this. I was a healthy 49 yo with some mild stomach discomfort. I noticed the onset of tinnitus earlier this year and I had Covid at the end of June. My first ‘flare-up’ with these symptoms was in August and I was eating gluten like normal. I had another flare-up in September and then got an upper endo at the end of September that showed possible celiac. My blood test came a week later. While I didn’t stop eating gluten before I had the blood test, I had cut back on food and gluten both. I had a flare-up with this symptoms after one week of gluten free but wasn’t being crazy careful. Then I had another flare-up this week. I think it might have been caused by Trader Joe’s baked tofu which I didn’t realize had wheat. But I don’t know if these flare-ups are caused by gluten or if there’s something else going on. I am food journaling and tracking all symptoms. I have lost 7 pounds in the last 10 days. 
    • trents
      Welcome to the forum, @Hmart! There are other medical conditions besides celiac disease that can cause villous atrophy as well as some medications and for some people, the dairy protein casein. So, your question is a valid one. Especially in view of the fact that your antibody testing was negative, though there are also some seronegative celiacs. So, do you get reactions every time you consume gluten? If you were to purposely consume a slice of bread would you be certain to develop the symptoms you describe?
    • klmgarland
    • DebJ14
      I only went on the multi vitamin AFTER a couple of year of high dose, targeted supplementation resolved most of my deficiencies.  I was on quite a cocktail of vitamins that was changed every 6 months as my deficiencies resolved.  Those that were determined to be genetic are still addressed with specific doses of those vitamins, minerals and amino acids. I have an update on my husband and his A Fib.  He ended up in the hospital in August 2025 when his A Fib would not convert.  He took the maximum dose of Flecainide allowed within a 24 hour period.  It was a nightmare experience!  They took him into the ER immediately.  They put in a line, drew blood, did an EKG and chest Xray all within minutes.  Never saw another human for 6 hours.  Never got any results, but obviously we could see he was still in A fib by watching the monitor.  They have the family sign up for text alerts at the ER desk.  So glad I did.  That is the only way we found out that he was being admitted.  About an hour after that text someone came to take him to his room on an observation floor.  We were there two hours before we saw another human being and believe it or not that was by zoom on the TV in the room.  It was admissions wanting to know his vaccine status and confirming his insurance, which we provided at the ER desk.  They said someone would be in and finally a nurse arrived.  He was told a hospitalist was in charge of his case.  Finally the NP for the hospitalist showed up and my husband literally blew his stack.  He got so angry and yelled at this poor woman, but it was exactly what he needed to convert himself to sinus rhythm while she was there.  They got an EKG machine and confirmed it.  She told him that they wanted to keep him overnight and would do an echo in the morning and they were concerned about a wound on his leg and wanted to do a doppler to make sure he did not have a DVT.  He agreed.  The echo showed everything fine, just as it was at his annual check up in June and there was no DVT.  A cardiologist finally showed up to discharge him and after reviewing his history said the A Fib was due to the Amoxicillan prescribed for his leg wound.  It both triggers A Fib and prevents the Flecainide from working.  His conversion coincided with the last dose of antibiotic getting out of his system.  So, make sure your PCP understands what antibiotics you can or cannot take if susceptible to A Fib.  This cardiologist (not his regular) wanted him on Metoprolol 25 mg and Pradaxa.  My husband told him that his cardiologist axed the idea of a beta blocker because his heart rate is already low.  Sure enough, it dropped to 42 on the Metoprolol and my husband felt horrible.  The pradaxa gave him a full body rash!  He went back to his cardiologist for follow up and his BP was fine and heart rate in the mid 50's.  He also axed the Pradaxa since my husband has low platelets, bruises easily and gets bloody noses just from Fish Oil  He suggested he take Black Cumin Seed Oil for inflammation.  He discovered that by taking the Black Seed oil, he can eat carbs and not go into A Fib, since it does such a good job of reducing inflammation.   Oh and I forgot to say the hospital bill was over $26,000.  Houston Methodist!  
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.